Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
2034696341
Device Listing 2034696341
Listing Summary
#
Listing key
2034696341
Premarket submission
K063675
Device
DIAGNOSTIC HYBRIDS' D3 DFA CHLAMYDIAE CULTURE CONFIRMATION KIT
Applicant
Diagnostic Hybrids, Inc.
Product code
LJP
Decision date
2007-09-24
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
13086
1528450
1000122536
QUIDEL CORPORATION
1
N
2020-04-25
2005 East State Street, Suite 100 ATHENS OH US 45701